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NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY

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Standard

NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY. / Olafsdottir, E. S.; Sorensen, A. M.; Cornett, Claus; Jaroszewski, J. W.

I: Journal of Organic Chemistry, Bind 56, Nr. 8, 1991, s. 2650-2655.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Olafsdottir, ES, Sorensen, AM, Cornett, C & Jaroszewski, JW 1991, 'NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY', Journal of Organic Chemistry, bind 56, nr. 8, s. 2650-2655.

APA

Olafsdottir, E. S., Sorensen, A. M., Cornett, C., & Jaroszewski, J. W. (1991). NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY. Journal of Organic Chemistry, 56(8), 2650-2655.

Vancouver

Olafsdottir ES, Sorensen AM, Cornett C, Jaroszewski JW. NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY. Journal of Organic Chemistry. 1991;56(8):2650-2655.

Author

Olafsdottir, E. S. ; Sorensen, A. M. ; Cornett, Claus ; Jaroszewski, J. W. / NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY. I: Journal of Organic Chemistry. 1991 ; Bind 56, Nr. 8. s. 2650-2655.

Bibtex

@article{04ccd5fee6ab47468ee383a9cbd94a15,
title = "NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY",
abstract = "Two stereoisomeric epoxycyclopentane cyanohydrin glucosides were isolated, along with several previously described cyclopentene cyanohydrin glucosides, from Passiflora suberosa L. (Passifloraceae) and Kiggelaria africana L. (Flacourtiaceae); they represent new members of a rare class of natural nonannellated cyclopentane derivatives. The new glucosides were shown, by NMR spectroscopy (including NOE measurements), X-ray crystallography, and enzymatic hydrolysis to the corresponding cyanohydrins, to be (1R,2R,3R,4R)- and (1S,2S,3S,4S)-1-(beta-D-glucopyranosyloxy)-2,3-epoxy-4-hydroxycyclopenta ne-1-carbonitrile and named suberin A and B, respectively. The crystal structure of suberin A was determined at 110 K and refined to R = 0.036 for 2198 unique reflections; the cyclopentane ring forms an envelope with C5 placed 0.41 angstrom away from the plane of the remaining four carbon atoms, and to the same side as the three oxygen substituents. In addition to the glucosides, two amides, (1S,2S,3R,4R)-2,3-epoxy-1,4-dihydroxycyclopentane-1-carboxamide and (1S,4R)-1,4-dihydroxy-2-cyclopentene-1-carboxamide, were isolated from P. suberosa and characterized; the amides are probably artefacts, and their formation represents a novel enzymatic transformation of plant cyanohydrins.",
keywords = "tetrapathaea-tetrandra cyanogenic glycosides tetraphyllin-b glucosides passifloraceae flacourtiaceae products pentenomycin intermediate antibiotics",
author = "Olafsdottir, {E. S.} and Sorensen, {A. M.} and Claus Cornett and Jaroszewski, {J. W.}",
year = "1991",
language = "Udefineret/Ukendt",
volume = "56",
pages = "2650--2655",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "8",

}

RIS

TY - JOUR

T1 - NATURAL CYCLOPENTANOID CYANOHYDRIN GLYCOSIDES .13. STRUCTURE DETERMINATION OF NATURAL EPOXYCYCLOPENTANES BY X-RAY CRYSTALLOGRAPHY AND NMR-SPECTROSCOPY

AU - Olafsdottir, E. S.

AU - Sorensen, A. M.

AU - Cornett, Claus

AU - Jaroszewski, J. W.

PY - 1991

Y1 - 1991

N2 - Two stereoisomeric epoxycyclopentane cyanohydrin glucosides were isolated, along with several previously described cyclopentene cyanohydrin glucosides, from Passiflora suberosa L. (Passifloraceae) and Kiggelaria africana L. (Flacourtiaceae); they represent new members of a rare class of natural nonannellated cyclopentane derivatives. The new glucosides were shown, by NMR spectroscopy (including NOE measurements), X-ray crystallography, and enzymatic hydrolysis to the corresponding cyanohydrins, to be (1R,2R,3R,4R)- and (1S,2S,3S,4S)-1-(beta-D-glucopyranosyloxy)-2,3-epoxy-4-hydroxycyclopenta ne-1-carbonitrile and named suberin A and B, respectively. The crystal structure of suberin A was determined at 110 K and refined to R = 0.036 for 2198 unique reflections; the cyclopentane ring forms an envelope with C5 placed 0.41 angstrom away from the plane of the remaining four carbon atoms, and to the same side as the three oxygen substituents. In addition to the glucosides, two amides, (1S,2S,3R,4R)-2,3-epoxy-1,4-dihydroxycyclopentane-1-carboxamide and (1S,4R)-1,4-dihydroxy-2-cyclopentene-1-carboxamide, were isolated from P. suberosa and characterized; the amides are probably artefacts, and their formation represents a novel enzymatic transformation of plant cyanohydrins.

AB - Two stereoisomeric epoxycyclopentane cyanohydrin glucosides were isolated, along with several previously described cyclopentene cyanohydrin glucosides, from Passiflora suberosa L. (Passifloraceae) and Kiggelaria africana L. (Flacourtiaceae); they represent new members of a rare class of natural nonannellated cyclopentane derivatives. The new glucosides were shown, by NMR spectroscopy (including NOE measurements), X-ray crystallography, and enzymatic hydrolysis to the corresponding cyanohydrins, to be (1R,2R,3R,4R)- and (1S,2S,3S,4S)-1-(beta-D-glucopyranosyloxy)-2,3-epoxy-4-hydroxycyclopenta ne-1-carbonitrile and named suberin A and B, respectively. The crystal structure of suberin A was determined at 110 K and refined to R = 0.036 for 2198 unique reflections; the cyclopentane ring forms an envelope with C5 placed 0.41 angstrom away from the plane of the remaining four carbon atoms, and to the same side as the three oxygen substituents. In addition to the glucosides, two amides, (1S,2S,3R,4R)-2,3-epoxy-1,4-dihydroxycyclopentane-1-carboxamide and (1S,4R)-1,4-dihydroxy-2-cyclopentene-1-carboxamide, were isolated from P. suberosa and characterized; the amides are probably artefacts, and their formation represents a novel enzymatic transformation of plant cyanohydrins.

KW - tetrapathaea-tetrandra cyanogenic glycosides tetraphyllin-b glucosides passifloraceae flacourtiaceae products pentenomycin intermediate antibiotics

M3 - Tidsskriftartikel

VL - 56

SP - 2650

EP - 2655

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 8

ER -

ID: 38062123